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人 80S 核糖体结构中化学修饰的可视化。

Visualization of chemical modifications in the human 80S ribosome structure.

机构信息

Centre for Integrative Biology (CBI), Department of Integrated Structural Biology, IGBMC, CNRS, Inserm, Université de Strasbourg, 1 rue Laurent Fries, 67404 Illkirch, France.

Institute of Genetics and of Molecular and Cellular Biology (IGBMC), 1 rue Laurent Fries, Illkirch, France.

出版信息

Nature. 2017 Nov 23;551(7681):472-477. doi: 10.1038/nature24482. Epub 2017 Nov 15.

Abstract

Chemical modifications of human ribosomal RNA (rRNA) are introduced during biogenesis and have been implicated in the dysregulation of protein synthesis, as is found in cancer and other diseases. However, their role in this phenomenon is unknown. Here we visualize more than 130 individual rRNA modifications in the three-dimensional structure of the human ribosome, explaining their structural and functional roles. In addition to a small number of universally conserved sites, we identify many eukaryote- or human-specific modifications and unique sites that form an extended shell in comparison to bacterial ribosomes, and which stabilize the RNA. Several of the modifications are associated with the binding sites of three ribosome-targeting antibiotics, or are associated with degenerate states in cancer, such as keto alkylations on nucleotide bases reminiscent of specialized ribosomes. This high-resolution structure of the human 80S ribosome paves the way towards understanding the role of epigenetic rRNA modifications in human diseases and suggests new possibilities for designing selective inhibitors and therapeutic drugs.

摘要

人类核糖体 RNA(rRNA)的化学修饰是在生物发生过程中引入的,并且与蛋白质合成的失调有关,如在癌症和其他疾病中发现的那样。然而,它们在这种现象中的作用尚不清楚。在这里,我们在人类核糖体的三维结构中可视化了 130 多个单独的 rRNA 修饰,解释了它们的结构和功能作用。除了少数普遍保守的位点外,我们还鉴定了许多真核生物或人类特异性修饰和独特的位点,与细菌核糖体相比,这些修饰和独特的位点形成了一个扩展的外壳,并稳定了 RNA。有几个修饰与三种核糖体靶向抗生素的结合位点相关,或者与癌症中的退化状态相关,例如核苷酸碱基上的酮烷基化类似于专门的核糖体。这种高分辨率的人类 80S 核糖体结构为理解表观遗传 rRNA 修饰在人类疾病中的作用铺平了道路,并为设计选择性抑制剂和治疗药物提供了新的可能性。

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